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Aldose reductase inhibitors from the leaves of Myrciaria dubia (H. B. & K.) McVaugh
Authors:H. Ueda   E. Kuroiwa   Y. Tachibana   K. Kawanishi   F. Ayala  M. Moriyasu
Affiliation:Kobe Pharmaceutical University, Higashinada-ku, Kobe, 658-8558 Japan.
Abstract:Ellagic acid (1) and its two derivatives, 4-O-methylellagic acid (2) and 4-(alpha-rhamnopyranosyl)ellagic acid (3) were isolated as inhibitors of aldose reductase (AR) from Myrciaria dubia (H. B. & K.) McVaugh. Compound 2 was the first isolated from the nature. Compound 3 showed the strongest inhibition against human recombinant AR (HRAR) and rat lens AR (RLAR). Inhibitory activity of compound 3 against HRAR (IC50 value = 4.1 x 10(-8) M) was 60 times more than that of quercetin (2.5 x 10(-6) M). The type of inhibition against HRAR was uncompetitive.
Keywords:Myrciaria dubia   Ellagic acid   4-O-methylellagic acid   4-(α  -rhamnopyranosyl)ellagic acid   Diabetes   Aldose reductase
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